DE10119681A1 - Schlagzähmodifizierte Blends aus Polyethylenenterephthalat und mindestens einem auf Dihydtoxydlarylcyclohexan basierenden Polycarbonat - Google Patents

Schlagzähmodifizierte Blends aus Polyethylenenterephthalat und mindestens einem auf Dihydtoxydlarylcyclohexan basierenden Polycarbonat

Info

Publication number: DE10119681A1
Authority: DE; Germany
Prior art keywords: weight; parts; component; polycarbonate; graft
Prior art date: 2001-04-20
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

DE10119681A

Other languages

German (de)

English (en)

Inventor

Thomas Braig

Detlev Joachimi

Matthias Bienmueller

Paul Friedemann

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bayer AG

Original Assignee

Bayer AG

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2001-04-20

Filing date

2001-04-20

Publication date

2002-10-24

2001-04-20 Application filed by Bayer AG filed Critical Bayer AG

2001-04-20 Priority to DE10119681A priority Critical patent/DE10119681A1/de

2002-04-08 Priority to JP2002584281A priority patent/JP2004526848A/ja

2002-04-08 Priority to RU2003133923/04A priority patent/RU2003133923A/ru

2002-04-08 Priority to MXPA03009478A priority patent/MXPA03009478A/es

2002-04-08 Priority to PCT/EP2002/003841 priority patent/WO2002086839A2/de

2002-04-08 Priority to BR0209043-0A priority patent/BR0209043A/pt

2002-04-08 Priority to CNA028124170A priority patent/CN1636035A/zh

2002-04-08 Priority to KR10-2003-7013611A priority patent/KR20030097831A/ko

2002-04-08 Priority to ES02732566T priority patent/ES2303550T3/es

2002-04-08 Priority to DE50212272T priority patent/DE50212272D1/de

2002-04-08 Priority to EP02732566A priority patent/EP1383836B1/de

2002-04-16 Priority to US10/123,273 priority patent/US20030022989A1/en

2002-04-18 Priority to ARP020101427A priority patent/AR033234A1/es

2002-10-24 Publication of DE10119681A1 publication Critical patent/DE10119681A1/de

2003-10-17 Priority to ZA200308088A priority patent/ZA200308088B/xx

Status Withdrawn legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 121
229920000515 polycarbonate Polymers 0.000 title claims abstract description 109
239000004417 polycarbonate Substances 0.000 title claims abstract description 109
-1 polyethylene terephthalate Polymers 0.000 title claims description 84
229920000139 polyethylene terephthalate Polymers 0.000 title claims description 37
239000005020 polyethylene terephthalate Substances 0.000 title claims description 23
238000002360 preparation method Methods 0.000 title description 5
239000012778 molding material Substances 0.000 title description 3
239000012779 reinforcing material Substances 0.000 claims abstract description 5
238000000465 moulding Methods 0.000 claims description 52
238000000034 method Methods 0.000 claims description 48
229920000642 polymer Polymers 0.000 claims description 38
229920000578 graft copolymer Polymers 0.000 claims description 31
239000000178 monomer Substances 0.000 claims description 30
239000000945 filler Substances 0.000 claims description 28
238000004519 manufacturing process Methods 0.000 claims description 24
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 23
239000000454 talc Substances 0.000 claims description 22
229910052623 talc Inorganic materials 0.000 claims description 22
125000003118 aryl group Chemical group 0.000 claims description 21
150000001875 compounds Chemical class 0.000 claims description 21
229920001971 elastomer Polymers 0.000 claims description 21
239000005060 rubber Substances 0.000 claims description 18
229910052500 inorganic mineral Inorganic materials 0.000 claims description 15
239000011707 mineral Substances 0.000 claims description 15
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 14
239000011265 semifinished product Substances 0.000 claims description 13
UMPGNGRIGSEMTC-UHFFFAOYSA-N 4-[1-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexyl]phenol Chemical compound C1C(C)CC(C)(C)CC1(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 UMPGNGRIGSEMTC-UHFFFAOYSA-N 0.000 claims description 9
WWNGFHNQODFIEX-UHFFFAOYSA-N buta-1,3-diene;methyl 2-methylprop-2-enoate;styrene Chemical compound C=CC=C.COC(=O)C(C)=C.C=CC1=CC=CC=C1 WWNGFHNQODFIEX-UHFFFAOYSA-N 0.000 claims description 7
QOHHOCDXTLIHPG-UHFFFAOYSA-N 4,4-diphenylcyclohexane-1,1-diol Chemical class C1CC(O)(O)CCC1(C=1C=CC=CC=1)C1=CC=CC=C1 QOHHOCDXTLIHPG-UHFFFAOYSA-N 0.000 claims description 6
230000009477 glass transition Effects 0.000 claims description 5
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 5
229920002554 vinyl polymer Polymers 0.000 claims description 5
229920009204 Methacrylate-butadiene-styrene Polymers 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 4
150000001252 acrylic acid derivatives Chemical class 0.000 claims description 2
150000001993 dienes Chemical class 0.000 claims description 2
150000001924 cycloalkanes Chemical class 0.000 claims 1
229920000428 triblock copolymer Polymers 0.000 claims 1
239000000463 material Substances 0.000 abstract description 11
229930185605 Bisphenol Natural products 0.000 description 34
VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 32
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 30
239000002585 base Substances 0.000 description 30
229920001400 block copolymer Polymers 0.000 description 25
125000004432 carbon atom Chemical group C* 0.000 description 22
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 20
125000000217 alkyl group Chemical group 0.000 description 19
239000002245 particle Substances 0.000 description 19
239000000654 additive Substances 0.000 description 15
239000012764 mineral filler Substances 0.000 description 15
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 14
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 14
235000010755 mineral Nutrition 0.000 description 14
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 13
239000004793 Polystyrene Substances 0.000 description 12
229920000728 polyester Polymers 0.000 description 12
229920002223 polystyrene Polymers 0.000 description 12
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 11
239000000155 melt Substances 0.000 description 11
239000006085 branching agent Substances 0.000 description 10
229920003023 plastic Polymers 0.000 description 10
239000004033 plastic Substances 0.000 description 10
239000010456 wollastonite Substances 0.000 description 10
229910052882 wollastonite Inorganic materials 0.000 description 10
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 9
229920001283 Polyalkylene terephthalate Polymers 0.000 description 9
239000002253 acid Substances 0.000 description 9
238000004132 cross linking Methods 0.000 description 9
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
229920001169 thermoplastic Polymers 0.000 description 9
239000004416 thermosoftening plastic Substances 0.000 description 9
238000005809 transesterification reaction Methods 0.000 description 9
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 8
238000005259 measurement Methods 0.000 description 8
239000003381 stabilizer Substances 0.000 description 8
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 7
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 7
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 7
238000002425 crystallisation Methods 0.000 description 7
230000008025 crystallization Effects 0.000 description 7
238000010422 painting Methods 0.000 description 7
229920001707 polybutylene terephthalate Polymers 0.000 description 7
238000012552 review Methods 0.000 description 7
239000000126 substance Substances 0.000 description 7
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 6
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
239000004609 Impact Modifier Substances 0.000 description 6
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
125000003342 alkenyl group Chemical group 0.000 description 6
QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 6
150000004649 carbonic acid derivatives Chemical class 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 6
150000002009 diols Chemical class 0.000 description 6
150000002148 esters Chemical class 0.000 description 6
238000007591 painting process Methods 0.000 description 6
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
239000005062 Polybutadiene Substances 0.000 description 5
150000001298 alcohols Chemical class 0.000 description 5
229920001577 copolymer Polymers 0.000 description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
238000005227 gel permeation chromatography Methods 0.000 description 5
229910052736 halogen Inorganic materials 0.000 description 5
150000002367 halogens Chemical class 0.000 description 5
239000006082 mold release agent Substances 0.000 description 5
150000002763 monocarboxylic acids Chemical class 0.000 description 5
229920002857 polybutadiene Polymers 0.000 description 5
238000006116 polymerization reaction Methods 0.000 description 5
BPILDHPJSYVNAF-UHFFFAOYSA-M sodium;diiodomethanesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C(I)I BPILDHPJSYVNAF-UHFFFAOYSA-M 0.000 description 5
BSWWXRFVMJHFBN-UHFFFAOYSA-N 2,4,6-tribromophenol Chemical compound OC1=C(Br)C=C(Br)C=C1Br BSWWXRFVMJHFBN-UHFFFAOYSA-N 0.000 description 4
UIAFKZKHHVMJGS-UHFFFAOYSA-N 2,4-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1O UIAFKZKHHVMJGS-UHFFFAOYSA-N 0.000 description 4
CJWNFAKWHDOUKL-UHFFFAOYSA-N 2-(2-phenylpropan-2-yl)phenol Chemical compound C=1C=CC=C(O)C=1C(C)(C)C1=CC=CC=C1 CJWNFAKWHDOUKL-UHFFFAOYSA-N 0.000 description 4
ZEKCYPANSOJWDH-UHFFFAOYSA-N 3,3-bis(4-hydroxy-3-methylphenyl)-1H-indol-2-one Chemical compound C1=C(O)C(C)=CC(C2(C3=CC=CC=C3NC2=O)C=2C=C(C)C(O)=CC=2)=C1 ZEKCYPANSOJWDH-UHFFFAOYSA-N 0.000 description 4
BRPSWMCDEYMRPE-UHFFFAOYSA-N 4-[1,1-bis(4-hydroxyphenyl)ethyl]phenol Chemical compound C=1C=C(O)C=CC=1C(C=1C=CC(O)=CC=1)(C)C1=CC=C(O)C=C1 BRPSWMCDEYMRPE-UHFFFAOYSA-N 0.000 description 4
ISAVYTVYFVQUDY-UHFFFAOYSA-N 4-tert-Octylphenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C=C1 ISAVYTVYFVQUDY-UHFFFAOYSA-N 0.000 description 4
QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 4
239000005995 Aluminium silicate Substances 0.000 description 4
239000005711 Benzoic acid Substances 0.000 description 4
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 4
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
239000003513 alkali Substances 0.000 description 4
125000005250 alkyl acrylate group Chemical group 0.000 description 4
235000012211 aluminium silicate Nutrition 0.000 description 4
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
235000010233 benzoic acid Nutrition 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
150000004651 carbonic acid esters Chemical class 0.000 description 4
239000003063 flame retardant Substances 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
239000001257 hydrogen Substances 0.000 description 4
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
125000005397 methacrylic acid ester group Chemical group 0.000 description 4
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
239000002667 nucleating agent Substances 0.000 description 4
239000003973 paint Substances 0.000 description 4
230000005501 phase interface Effects 0.000 description 4
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
239000000047 product Substances 0.000 description 4
239000002994 raw material Substances 0.000 description 4
150000004756 silanes Chemical class 0.000 description 4
238000003786 synthesis reaction Methods 0.000 description 4
238000005199 ultracentrifugation Methods 0.000 description 4
YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 3
VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 3
229920001634 Copolyester Polymers 0.000 description 3
239000004641 Diallyl-phthalate Substances 0.000 description 3
229920002633 Kraton (polymer) Polymers 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
125000005396 acrylic acid ester group Chemical group 0.000 description 3
239000002318 adhesion promoter Substances 0.000 description 3
QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 3
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical group OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
238000013329 compounding Methods 0.000 description 3
239000000806 elastomer Substances 0.000 description 3
239000004744 fabric Substances 0.000 description 3
150000002500 ions Chemical class 0.000 description 3
150000002576 ketones Chemical class 0.000 description 3
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
150000002989 phenols Chemical class 0.000 description 3
150000003018 phosphorus compounds Chemical class 0.000 description 3
239000000049 pigment Substances 0.000 description 3
229920003251 poly(α-methylstyrene) Polymers 0.000 description 3
229920001195 polyisoprene Polymers 0.000 description 3
229920000166 polytrimethylene carbonate Polymers 0.000 description 3
238000012545 processing Methods 0.000 description 3
FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 description 3
238000009757 thermoplastic moulding Methods 0.000 description 3
239000004408 titanium dioxide Substances 0.000 description 3
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 2
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
FQXGHZNSUOHCLO-UHFFFAOYSA-N 2,2,4,4-tetramethyl-1,3-cyclobutanediol Chemical compound CC1(C)C(O)C(C)(C)C1O FQXGHZNSUOHCLO-UHFFFAOYSA-N 0.000 description 2
DFOLZQISJZKWBT-UHFFFAOYSA-N 2,3-dihydro-1h-indene;phenol Chemical class OC1=CC=CC=C1.OC1=CC=CC=C1.C1=CC=C2CCCC2=C1 DFOLZQISJZKWBT-UHFFFAOYSA-N 0.000 description 2
BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 2
VPVTXVHUJHGOCM-UHFFFAOYSA-N 2,4-bis[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C=1C=C(O)C(C(C)(C)C=2C=CC(O)=CC=2)=CC=1C(C)(C)C1=CC=C(O)C=C1 VPVTXVHUJHGOCM-UHFFFAOYSA-N 0.000 description 2
MAQOZOILPAMFSW-UHFFFAOYSA-N 2,6-bis[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=C(CC=3C(=CC=C(C)C=3)O)C=C(C)C=2)O)=C1 MAQOZOILPAMFSW-UHFFFAOYSA-N 0.000 description 2
KAIRTVANLJFYQS-UHFFFAOYSA-N 2-(3,5-dimethylheptyl)phenol Chemical compound CCC(C)CC(C)CCC1=CC=CC=C1O KAIRTVANLJFYQS-UHFFFAOYSA-N 0.000 description 2
RWLALWYNXFYRGW-UHFFFAOYSA-N 2-Ethyl-1,3-hexanediol Chemical compound CCCC(O)C(CC)CO RWLALWYNXFYRGW-UHFFFAOYSA-N 0.000 description 2
YQPCHPBGAALCRT-UHFFFAOYSA-N 2-[1-(carboxymethyl)cyclohexyl]acetic acid Chemical compound OC(=O)CC1(CC(O)=O)CCCCC1 YQPCHPBGAALCRT-UHFFFAOYSA-N 0.000 description 2
ICPXIRMAMWRMAD-UHFFFAOYSA-N 2-[3-[2-[3-(2-hydroxyethoxy)phenyl]propan-2-yl]phenoxy]ethanol Chemical compound C=1C=CC(OCCO)=CC=1C(C)(C)C1=CC=CC(OCCO)=C1 ICPXIRMAMWRMAD-UHFFFAOYSA-N 0.000 description 2
WTPYFJNYAMXZJG-UHFFFAOYSA-N 2-[4-(2-hydroxyethoxy)phenoxy]ethanol Chemical compound OCCOC1=CC=C(OCCO)C=C1 WTPYFJNYAMXZJG-UHFFFAOYSA-N 0.000 description 2
ZDWSNKPLZUXBPE-UHFFFAOYSA-N 3,5-ditert-butylphenol Chemical compound CC(C)(C)C1=CC(O)=CC(C(C)(C)C)=C1 ZDWSNKPLZUXBPE-UHFFFAOYSA-N 0.000 description 2
CPHURRLSZSRQFS-UHFFFAOYSA-N 3-[4-[2-[4-(3-hydroxypropoxy)phenyl]propan-2-yl]phenoxy]propan-1-ol Chemical compound C=1C=C(OCCCO)C=CC=1C(C)(C)C1=CC=C(OCCCO)C=C1 CPHURRLSZSRQFS-UHFFFAOYSA-N 0.000 description 2
CUAUDSWILJWDOD-UHFFFAOYSA-N 4-(3,5-dimethylheptyl)phenol Chemical compound CCC(C)CC(C)CCC1=CC=C(O)C=C1 CUAUDSWILJWDOD-UHFFFAOYSA-N 0.000 description 2
KJWMCPYEODZESQ-UHFFFAOYSA-N 4-Dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C=C1 KJWMCPYEODZESQ-UHFFFAOYSA-N 0.000 description 2
CDBAMNGURPMUTG-UHFFFAOYSA-N 4-[2-(4-hydroxycyclohexyl)propan-2-yl]cyclohexan-1-ol Chemical compound C1CC(O)CCC1C(C)(C)C1CCC(O)CC1 CDBAMNGURPMUTG-UHFFFAOYSA-N 0.000 description 2
XJGTVJRTDRARGO-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)propan-2-yl]benzene-1,3-diol Chemical compound C=1C=C(O)C=C(O)C=1C(C)(C)C1=CC=C(O)C=C1 XJGTVJRTDRARGO-UHFFFAOYSA-N 0.000 description 2
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239000012963 UV stabilizer Substances 0.000 description 1
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VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical group C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 description 1
150000001642 boronic acid derivatives Chemical class 0.000 description 1
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125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
239000004917 carbon fiber Substances 0.000 description 1
JYYOBHFYCIDXHH-UHFFFAOYSA-N carbonic acid;hydrate Chemical class O.OC(O)=O JYYOBHFYCIDXHH-UHFFFAOYSA-N 0.000 description 1
150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
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239000011248 coating agent Substances 0.000 description 1
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229920003244 diene elastomer Polymers 0.000 description 1
HANKSFAYJLDDKP-UHFFFAOYSA-N dihydrodicyclopentadiene Chemical compound C12CC=CC2C2CCC1C2 HANKSFAYJLDDKP-UHFFFAOYSA-N 0.000 description 1
239000000539 dimer Substances 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000003618 dip coating Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004870 electrical engineering Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
PFBWBEXCUGKYKO-UHFFFAOYSA-N ethene;n-octadecyloctadecan-1-amine Chemical compound C=C.CCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCC PFBWBEXCUGKYKO-UHFFFAOYSA-N 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000011152 fibreglass Substances 0.000 description 1
239000000796 flavoring agent Substances 0.000 description 1
235000019634 flavors Nutrition 0.000 description 1
239000011888 foil Substances 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
125000001188 haloalkyl group Chemical group 0.000 description 1
230000026030 halogenation Effects 0.000 description 1
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150000002430 hydrocarbons Chemical class 0.000 description 1
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238000002347 injection Methods 0.000 description 1
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ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
238000004898 kneading Methods 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
150000004668 long chain fatty acids Chemical class 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
239000000347 magnesium hydroxide Substances 0.000 description 1
229960000816 magnesium hydroxide Drugs 0.000 description 1
229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
235000012254 magnesium hydroxide Nutrition 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 description 1
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239000012170 montan wax Substances 0.000 description 1
239000002071 nanotube Substances 0.000 description 1
125000004957 naphthylene group Chemical group 0.000 description 1
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150000002830 nitrogen compounds Chemical class 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000002897 organic nitrogen compounds Chemical class 0.000 description 1
RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
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CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
HCTVWSOKIJULET-LQDWTQKMSA-M phenoxymethylpenicillin potassium Chemical compound [K+].N([C@H]1[C@H]2SC([C@@H](N2C1=O)C([O-])=O)(C)C)C(=O)COC1=CC=CC=C1 HCTVWSOKIJULET-LQDWTQKMSA-M 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
XZTOTRSSGPPNTB-UHFFFAOYSA-N phosphono dihydrogen phosphate;1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(N)=N1.OP(O)(=O)OP(O)(O)=O XZTOTRSSGPPNTB-UHFFFAOYSA-N 0.000 description 1
XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 description 1
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920006324 polyoxymethylene Polymers 0.000 description 1
239000001205 polyphosphate Substances 0.000 description 1
235000011176 polyphosphates Nutrition 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
238000011417 postcuring Methods 0.000 description 1
239000002243 precursor Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
230000002787 reinforcement Effects 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
210000003660 reticulum Anatomy 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
150000003902 salicylic acid esters Chemical class 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
HHJJPFYGIRKQOM-UHFFFAOYSA-N sodium;oxido-oxo-phenylphosphanium Chemical compound [Na+].[O-][P+](=O)C1=CC=CC=C1 HHJJPFYGIRKQOM-UHFFFAOYSA-N 0.000 description 1
239000002904 solvent Substances 0.000 description 1
229940071182 stannate Drugs 0.000 description 1
125000005402 stannate group Chemical group 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
238000012360 testing method Methods 0.000 description 1
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
238000002076 thermal analysis method Methods 0.000 description 1
229920002725 thermoplastic elastomer Polymers 0.000 description 1
150000003606 tin compounds Chemical class 0.000 description 1
210000002105 tongue Anatomy 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 description 1
235000013799 ultramarine blue Nutrition 0.000 description 1
239000002966 varnish Substances 0.000 description 1
238000003466 welding Methods 0.000 description 1
150000003752 zinc compounds Chemical class 0.000 description 1
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/04—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Manufacture Of Macromolecular Shaped Articles (AREA)

DE10119681A 2001-04-20 2001-04-20 Schlagzähmodifizierte Blends aus Polyethylenenterephthalat und mindestens einem auf Dihydtoxydlarylcyclohexan basierenden Polycarbonat Withdrawn DE10119681A1 (de)

Priority Applications (14)

Application Number	Priority Date	Filing Date	Title
DE10119681A DE10119681A1 (de)	2001-04-20	2001-04-20	Schlagzähmodifizierte Blends aus Polyethylenenterephthalat und mindestens einem auf Dihydtoxydlarylcyclohexan basierenden Polycarbonat
KR10-2003-7013611A KR20030097831A (ko)	2001-04-20	2002-04-08	폴리에틸렌테레프탈레이트 및 1종 이상의디히드록시디아릴시클로헥산 기재 폴리카르보네이트로제조된 내충격성 개질 블렌드
ES02732566T ES2303550T3 (es)	2001-04-20	2002-04-08	Mixturas modificadas a la resiliencia constituidas por tereftalato de polietileno y por, al menos, un policarbonato basado en dihidroxidiarilciclohexano.
MXPA03009478A MXPA03009478A (es)	2001-04-20	2002-04-08	Mezclas con resistencia al impacto modificada de poli (tereftalato de etileno) y al menos un policarbonato basado en dihidroxidiarilciclohexano.
PCT/EP2002/003841 WO2002086839A2 (de)	2001-04-20	2002-04-08	Schlagzähmodifizierte blends aus polyethylenterephthalat und mindestens einem auf dihydroxydiarylcyclohexan basierenden polycarbonat
BR0209043-0A BR0209043A (pt)	2001-04-20	2002-04-08	Misturas de tereftalato de polietileno e pelo menos um policarbonato à base de dihidroxidiarilciclohexano modificadas tenazes ao choque
CNA028124170A CN1636035A (zh)	2001-04-20	2002-04-08	聚对苯二甲酸乙二醇酯和至少一种基于二羟基二芳基环己烷的聚碳酸酯的抗冲改性共混物
JP2002584281A JP2004526848A (ja)	2001-04-20	2002-04-08	ポリエチレンテレフタレートと少なくとも１種のジヒドロキシジアリールシクロヘキサン系ポリカーボネートを含有する衝撃変性された組成物
RU2003133923/04A RU2003133923A (ru)	2001-04-20	2002-04-08	Композиции с модифицированной ударной вязкостью из полиэтилентерефталата и, по меньшей мере, одного поликарбоната на основе дигидроксидиарилциклогексана
DE50212272T DE50212272D1 (de)	2001-04-20	2002-04-08	Schlagzähmodifizierte blends aus polyethylenterephthalat und mindestens einem auf dihydroxydiarylcyclohexan basierenden polycarbonat
EP02732566A EP1383836B1 (de)	2001-04-20	2002-04-08	Schlagzähmodifizierte blends aus polyethylenterephthalat und mindestens einem auf dihydroxydiarylcyclohexan basierenden polycarbonat
US10/123,273 US20030022989A1 (en)	2001-04-20	2002-04-16	Impact-modified molding compositions of polyethylene terephthalate and dihydroxydiarylcyclohexane-based polycarbonate
ARP020101427A AR033234A1 (es)	2001-04-20	2002-04-18	Composiciones de moldeo modificadas en su resistencia al impacto de tereftalato de polietileno y policarbonato basado en dihidroxidiarilciclohexano
ZA200308088A ZA200308088B (en)	2001-04-20	2003-10-17	Impact resistant modified blends made of polyethylenterephthalate and at least one polycarbonate based on dihydroxydiarylcyclohexane.

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE10119681A DE10119681A1 (de)	2001-04-20	2001-04-20	Schlagzähmodifizierte Blends aus Polyethylenenterephthalat und mindestens einem auf Dihydtoxydlarylcyclohexan basierenden Polycarbonat

Publications (1)

Publication Number	Publication Date
DE10119681A1 true DE10119681A1 (de)	2002-10-24

Family

ID=7682293

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DE10119681A Withdrawn DE10119681A1 (de)	2001-04-20	2001-04-20	Schlagzähmodifizierte Blends aus Polyethylenenterephthalat und mindestens einem auf Dihydtoxydlarylcyclohexan basierenden Polycarbonat
DE50212272T Expired - Lifetime DE50212272D1 (de)	2001-04-20	2002-04-08	Schlagzähmodifizierte blends aus polyethylenterephthalat und mindestens einem auf dihydroxydiarylcyclohexan basierenden polycarbonat

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
DE50212272T Expired - Lifetime DE50212272D1 (de)	2001-04-20	2002-04-08	Schlagzähmodifizierte blends aus polyethylenterephthalat und mindestens einem auf dihydroxydiarylcyclohexan basierenden polycarbonat

Country Status (13)

Country	Link
US (1)	US20030022989A1 (es)
EP (1)	EP1383836B1 (es)
JP (1)	JP2004526848A (es)
KR (1)	KR20030097831A (es)
CN (1)	CN1636035A (es)
AR (1)	AR033234A1 (es)
BR (1)	BR0209043A (es)
DE (2)	DE10119681A1 (es)
ES (1)	ES2303550T3 (es)
MX (1)	MXPA03009478A (es)
RU (1)	RU2003133923A (es)
WO (1)	WO2002086839A2 (es)
ZA (1)	ZA200308088B (es)

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US7759449B2 (en) *	2000-12-15	2010-07-20	Wellman, Inc.	Methods for introducing additives into polyethylene terephthalate
DE10256316A1 (de) *	2002-12-03	2004-06-24	Bayer Ag	Polycarbonat-Formmassen
DE10300110A1 (de) *	2003-01-07	2004-07-15	Bayer Ag	Homogen durchgefärbte Zusammensetzungen auf Basis schlagzähmodifizierten Polyalkylenterephthalat/Polycarbonat Blends
ATE453678T1 (de) †	2003-05-12	2010-01-15	Teijin Chemicals Ltd	Flächenförmiges fensterelement und fensteraufbau
US20070112144A1 (en) *	2004-04-12	2007-05-17	Viswanathan Kalyanaraman	Method for decreasing gloss in molded article
US20050228130A1 (en) *	2004-04-12	2005-10-13	General Electric Company	Thermoplastic composition providing a low gloss, textured surface, and method
US8268916B2 (en) *	2006-09-25	2012-09-18	Federal-Mogul World Wide, Inc.	Flame-retardant compound and method of forming a continuous material therefrom
US20080227914A1 (en) *	2007-03-16	2008-09-18	Bfs Diversified Products, Llc	Recycled building material and method thereof
JP5342804B2 (ja) *	2008-05-07	2013-11-13	出光興産株式会社	芳香族ポリカーボネート樹脂組成物およびその成形体
DE102009039121A1 (de) *	2009-08-28	2011-03-03	Bayer Materialscience Ag	Erzeugnisse mit verbesserter Flammwidrigkeit
US9043829B2 (en) *	2009-10-07	2015-05-26	At&T Intellectual Property I, Lp	Synchronization of user interactive events with on-screen events during playback of multimedia stream
DE102009058099A1 (de) *	2009-12-12	2011-06-16	Bayer Materialscience Ag	Polycarbonatblends mit hoher Wärmeformbeständigkeit und verbesserten Oberflächeneigenschaften
US8697786B2 (en)	2010-06-16	2014-04-15	Federal Mogul Powertrain, Inc.	Flame-retardant compound, continuous materials and products constructed therefrom and methods of manufacture thereof
US20150086800A1 (en) *	2013-09-04	2015-03-26	Roderick Hughes	Stress-Resistant Extrudates
JP6655537B2 (ja)	2014-08-14	2020-02-26	株式会社カネカ	熱可塑性樹脂組成物およびその成形体
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2001
- 2001-04-20 DE DE10119681A patent/DE10119681A1/de not_active Withdrawn
2002
- 2002-04-08 EP EP02732566A patent/EP1383836B1/de not_active Expired - Lifetime
- 2002-04-08 ES ES02732566T patent/ES2303550T3/es not_active Expired - Lifetime
- 2002-04-08 WO PCT/EP2002/003841 patent/WO2002086839A2/de not_active Ceased
- 2002-04-08 JP JP2002584281A patent/JP2004526848A/ja active Pending
- 2002-04-08 CN CNA028124170A patent/CN1636035A/zh active Pending
- 2002-04-08 BR BR0209043-0A patent/BR0209043A/pt not_active IP Right Cessation
- 2002-04-08 RU RU2003133923/04A patent/RU2003133923A/ru not_active Application Discontinuation
- 2002-04-08 MX MXPA03009478A patent/MXPA03009478A/es not_active Application Discontinuation
- 2002-04-08 KR KR10-2003-7013611A patent/KR20030097831A/ko not_active Ceased
- 2002-04-08 DE DE50212272T patent/DE50212272D1/de not_active Expired - Lifetime
- 2002-04-16 US US10/123,273 patent/US20030022989A1/en not_active Abandoned
- 2002-04-18 AR ARP020101427A patent/AR033234A1/es not_active Application Discontinuation
2003
- 2003-10-17 ZA ZA200308088A patent/ZA200308088B/xx unknown

Also Published As

Publication number	Publication date
DE50212272D1 (de)	2008-06-26
US20030022989A1 (en)	2003-01-30
EP1383836B1 (de)	2008-05-14
JP2004526848A (ja)	2004-09-02
EP1383836A2 (de)	2004-01-28
MXPA03009478A (es)	2004-05-24
ZA200308088B (en)	2004-10-18
ES2303550T3 (es)	2008-08-16
WO2002086839A2 (de)	2002-10-31
BR0209043A (pt)	2004-08-10
CN1636035A (zh)	2005-07-06
WO2002086839A3 (de)	2003-02-06
AR033234A1 (es)	2003-12-10
RU2003133923A (ru)	2005-05-10
KR20030097831A (ko)	2003-12-31

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